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Interrogation of Related Clinical Pan-Azole-Resistant Aspergillus fumigatus Strains: G138C, Y431C, and G434C Single Nucleotide Polymorphisms in cyp51A, Upregulation of cyp51A, and Integration and Activation of Transposon Atf1 in the cyp51A Promoter
Multiple Aspergillus fumigatus isolates from a patient with two aspergillomas complicating chronic pulmonary aspergillosis were pan-azole resistant. Microsatellite typing was identical for all isolates despite major phenotypic and some growth rate differences. Three different cyp51A mutations were f...
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Published in: | Antimicrobial Agents and Chemotherapy 2011-11, Vol.55 (11), p.5113-5121 |
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description | Multiple Aspergillus fumigatus isolates from a patient with two aspergillomas complicating chronic pulmonary aspergillosis were pan-azole resistant. Microsatellite typing was identical for all isolates despite major phenotypic and some growth rate differences. Three different cyp51A mutations were found (G138C, Y431C, and G434C), of which the first two were demonstrated by heterologous expression in a hypersusceptible Saccharomyces cerevisiae strain to be at least partly responsible for elevated MICs. cyp51A and cyp51B gene duplication was excluded, but increased expression of cyp51A was demonstrated in three isolates selected for additional study (7-to 13-fold increases). In the isolate with the greatest cyp51A expression, an Aft1 transposon was found inserted 370 bp upstream of the start codon of the cyp51A gene, an integration location never previously demonstrated in ASPERGILLUS: Two transcription start sites were identified at 49 and 136 bp upstream of the start codon. The role of the Aft1 transposon, if any, in modulating cyp51A expression remains to be established. Increased mRNA expression of the transporters AfuMDR1 and AfuMDR4 also was demonstrated in some isolates, which could contribute to azole resistance or simply represent a stress response. The diversity of confirmed and possible azole resistance mechanisms demonstrated in a single series of isogenic isolates is remarkable, indicating the ability of A. fumigatus to adapt in the clinical setting. |
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Microsatellite typing was identical for all isolates despite major phenotypic and some growth rate differences. Three different cyp51A mutations were found (G138C, Y431C, and G434C), of which the first two were demonstrated by heterologous expression in a hypersusceptible Saccharomyces cerevisiae strain to be at least partly responsible for elevated MICs. cyp51A and cyp51B gene duplication was excluded, but increased expression of cyp51A was demonstrated in three isolates selected for additional study (7-to 13-fold increases). In the isolate with the greatest cyp51A expression, an Aft1 transposon was found inserted 370 bp upstream of the start codon of the cyp51A gene, an integration location never previously demonstrated in ASPERGILLUS: Two transcription start sites were identified at 49 and 136 bp upstream of the start codon. The role of the Aft1 transposon, if any, in modulating cyp51A expression remains to be established. Increased mRNA expression of the transporters AfuMDR1 and AfuMDR4 also was demonstrated in some isolates, which could contribute to azole resistance or simply represent a stress response. The diversity of confirmed and possible azole resistance mechanisms demonstrated in a single series of isogenic isolates is remarkable, indicating the ability of A. fumigatus to adapt in the clinical setting.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.00517-11</identifier><identifier>PMID: 21876055</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Antifungal Agents - pharmacology ; aspergillosis ; Aspergillus fumigatus ; Aspergillus fumigatus - drug effects ; Aspergillus fumigatus - genetics ; Aspergillus fumigatus - metabolism ; Azoles ; Azoles - pharmacology ; cytochrome P-450 ; Cytochrome P-450 Enzyme System ; Cytochrome P-450 Enzyme System - genetics ; Cytochrome P-450 Enzyme System - metabolism ; DNA Transposable Elements - genetics ; Drug Resistance, Fungal - genetics ; Fungal Proteins ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; gene duplication ; gene expression ; gene expression regulation ; genes ; Mechanisms of Resistance ; messenger RNA ; microsatellite repeats ; multiple drug resistance ; patients ; Polymorphism, Single Nucleotide ; Polymorphism, Single Nucleotide - genetics ; promoter regions ; Promoter Regions, Genetic - genetics ; resistance mechanisms ; Saccharomyces cerevisiae ; single nucleotide polymorphism ; start codon ; stress response ; transporters ; transposons</subject><ispartof>Antimicrobial Agents and Chemotherapy, 2011-11, Vol.55 (11), p.5113-5121</ispartof><rights>Copyright © 2011, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2011, American Society for Microbiology. All Rights Reserved. 2011 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a468t-7f9ab96a9248f3b913fa8708395ca4ce47c1c5f22743e1bdb8d52d1b215552723</citedby><cites>FETCH-LOGICAL-a468t-7f9ab96a9248f3b913fa8708395ca4ce47c1c5f22743e1bdb8d52d1b215552723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/AAC.00517-11$$EPDF$$P50$$Gasm2$$H</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/AAC.00517-11$$EHTML$$P50$$Gasm2$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,52751,52752,52753,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21876055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albarrag, Ahmed M</creatorcontrib><creatorcontrib>Anderson, Michael J</creatorcontrib><creatorcontrib>Howard, Susan J</creatorcontrib><creatorcontrib>Robson, Geoff D</creatorcontrib><creatorcontrib>Warn, Peter A</creatorcontrib><creatorcontrib>Sanglard, Dominique</creatorcontrib><creatorcontrib>Denning, David W</creatorcontrib><title>Interrogation of Related Clinical Pan-Azole-Resistant Aspergillus fumigatus Strains: G138C, Y431C, and G434C Single Nucleotide Polymorphisms in cyp51A, Upregulation of cyp51A, and Integration and Activation of Transposon Atf1 in the cyp51A Promoter</title><title>Antimicrobial Agents and Chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>Multiple Aspergillus fumigatus isolates from a patient with two aspergillomas complicating chronic pulmonary aspergillosis were pan-azole resistant. Microsatellite typing was identical for all isolates despite major phenotypic and some growth rate differences. Three different cyp51A mutations were found (G138C, Y431C, and G434C), of which the first two were demonstrated by heterologous expression in a hypersusceptible Saccharomyces cerevisiae strain to be at least partly responsible for elevated MICs. cyp51A and cyp51B gene duplication was excluded, but increased expression of cyp51A was demonstrated in three isolates selected for additional study (7-to 13-fold increases). In the isolate with the greatest cyp51A expression, an Aft1 transposon was found inserted 370 bp upstream of the start codon of the cyp51A gene, an integration location never previously demonstrated in ASPERGILLUS: Two transcription start sites were identified at 49 and 136 bp upstream of the start codon. The role of the Aft1 transposon, if any, in modulating cyp51A expression remains to be established. Increased mRNA expression of the transporters AfuMDR1 and AfuMDR4 also was demonstrated in some isolates, which could contribute to azole resistance or simply represent a stress response. The diversity of confirmed and possible azole resistance mechanisms demonstrated in a single series of isogenic isolates is remarkable, indicating the ability of A. fumigatus to adapt in the clinical setting.</description><subject>Antifungal Agents - pharmacology</subject><subject>aspergillosis</subject><subject>Aspergillus fumigatus</subject><subject>Aspergillus fumigatus - drug effects</subject><subject>Aspergillus fumigatus - genetics</subject><subject>Aspergillus fumigatus - metabolism</subject><subject>Azoles</subject><subject>Azoles - pharmacology</subject><subject>cytochrome P-450</subject><subject>Cytochrome P-450 Enzyme System</subject><subject>Cytochrome P-450 Enzyme System - genetics</subject><subject>Cytochrome P-450 Enzyme System - metabolism</subject><subject>DNA Transposable Elements - genetics</subject><subject>Drug Resistance, Fungal - genetics</subject><subject>Fungal Proteins</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>gene duplication</subject><subject>gene expression</subject><subject>gene expression regulation</subject><subject>genes</subject><subject>Mechanisms of Resistance</subject><subject>messenger RNA</subject><subject>microsatellite repeats</subject><subject>multiple drug resistance</subject><subject>patients</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>promoter regions</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>resistance mechanisms</subject><subject>Saccharomyces cerevisiae</subject><subject>single nucleotide polymorphism</subject><subject>start codon</subject><subject>stress response</subject><subject>transporters</subject><subject>transposons</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kkGP1CAYhhujccfVm2clXozJdIUWWurBpGl03GSjk52dgyfCtLTDhkIX6Jrxl3uU2tmJHjzBBw8PH-SNopcIXiCU0PdlWV1ASFAeI_QoWiBY0DgjRfY4WkCYZTGmEJ9Fz5y7haEmBXwanSWI5hkkZBH9utReWGs67qXRwLTgWijuRQMqJbWsuQJrruPyp1EivhZOOs-1B6UbhO2kUqMD7djLcDzMNt5yqd0HsEIprZbgO05RGLhuwAqnuAIbqTslwNexVsJ42QiwNurQGzvspesdkBrUh4Ggcgm2gxXdqE5tPaxPsqnnzs5bU13WXt6fyBvLtRuMC1XpWzRJ_V4cBWBtTW_Ck59HT1qunHhxHM-j7edPN9WX-Orb6rIqr2KOM-rjvC34rsh4kWDaprsCpS2nOaRpQWqOa4HzGtWkTZIcpwLtmh1tSNKgXYIIIUmepOfRx9k7jLteNLXQ4ZMUG6zsuT0wwyX7d0fLPevMPUtRQSDGQfD2KLDmbhTOs166WijFtTCjY7SgNKWUZoFczmRtjXNWtKdbEGRTVljICvuTlVAG_N2Mc9cn7NaMVoeP-B_76u9XnMQPQQrAmxnYy27_Q1rBgpVxXjNCgoCRIAnQ6xlquWG8s9Kx7SaBiMApmhjl6W-SU90Z</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Albarrag, Ahmed M</creator><creator>Anderson, Michael J</creator><creator>Howard, Susan J</creator><creator>Robson, Geoff D</creator><creator>Warn, Peter A</creator><creator>Sanglard, Dominique</creator><creator>Denning, David W</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20111101</creationdate><title>Interrogation of Related Clinical Pan-Azole-Resistant Aspergillus fumigatus Strains: G138C, Y431C, and G434C Single Nucleotide Polymorphisms in cyp51A, Upregulation of cyp51A, and Integration and Activation of Transposon Atf1 in the cyp51A Promoter</title><author>Albarrag, Ahmed M ; Anderson, Michael J ; Howard, Susan J ; Robson, Geoff D ; Warn, Peter A ; Sanglard, Dominique ; Denning, David W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a468t-7f9ab96a9248f3b913fa8708395ca4ce47c1c5f22743e1bdb8d52d1b215552723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Antifungal Agents - pharmacology</topic><topic>aspergillosis</topic><topic>Aspergillus fumigatus</topic><topic>Aspergillus fumigatus - drug effects</topic><topic>Aspergillus fumigatus - genetics</topic><topic>Aspergillus fumigatus - metabolism</topic><topic>Azoles</topic><topic>Azoles - pharmacology</topic><topic>cytochrome P-450</topic><topic>Cytochrome P-450 Enzyme System</topic><topic>Cytochrome P-450 Enzyme System - genetics</topic><topic>Cytochrome P-450 Enzyme System - metabolism</topic><topic>DNA Transposable Elements - genetics</topic><topic>Drug Resistance, Fungal - genetics</topic><topic>Fungal Proteins</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>gene duplication</topic><topic>gene expression</topic><topic>gene expression regulation</topic><topic>genes</topic><topic>Mechanisms of Resistance</topic><topic>messenger RNA</topic><topic>microsatellite repeats</topic><topic>multiple drug resistance</topic><topic>patients</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>promoter regions</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>resistance mechanisms</topic><topic>Saccharomyces cerevisiae</topic><topic>single nucleotide polymorphism</topic><topic>start codon</topic><topic>stress response</topic><topic>transporters</topic><topic>transposons</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Albarrag, Ahmed M</creatorcontrib><creatorcontrib>Anderson, Michael J</creatorcontrib><creatorcontrib>Howard, Susan J</creatorcontrib><creatorcontrib>Robson, Geoff D</creatorcontrib><creatorcontrib>Warn, Peter A</creatorcontrib><creatorcontrib>Sanglard, Dominique</creatorcontrib><creatorcontrib>Denning, David W</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial Agents and Chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Albarrag, Ahmed M</au><au>Anderson, Michael J</au><au>Howard, Susan J</au><au>Robson, Geoff D</au><au>Warn, Peter A</au><au>Sanglard, Dominique</au><au>Denning, David W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interrogation of Related Clinical Pan-Azole-Resistant Aspergillus fumigatus Strains: G138C, Y431C, and G434C Single Nucleotide Polymorphisms in cyp51A, Upregulation of cyp51A, and Integration and Activation of Transposon Atf1 in the cyp51A Promoter</atitle><jtitle>Antimicrobial Agents and Chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>55</volume><issue>11</issue><spage>5113</spage><epage>5121</epage><pages>5113-5121</pages><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Multiple Aspergillus fumigatus isolates from a patient with two aspergillomas complicating chronic pulmonary aspergillosis were pan-azole resistant. Microsatellite typing was identical for all isolates despite major phenotypic and some growth rate differences. Three different cyp51A mutations were found (G138C, Y431C, and G434C), of which the first two were demonstrated by heterologous expression in a hypersusceptible Saccharomyces cerevisiae strain to be at least partly responsible for elevated MICs. cyp51A and cyp51B gene duplication was excluded, but increased expression of cyp51A was demonstrated in three isolates selected for additional study (7-to 13-fold increases). In the isolate with the greatest cyp51A expression, an Aft1 transposon was found inserted 370 bp upstream of the start codon of the cyp51A gene, an integration location never previously demonstrated in ASPERGILLUS: Two transcription start sites were identified at 49 and 136 bp upstream of the start codon. The role of the Aft1 transposon, if any, in modulating cyp51A expression remains to be established. Increased mRNA expression of the transporters AfuMDR1 and AfuMDR4 also was demonstrated in some isolates, which could contribute to azole resistance or simply represent a stress response. The diversity of confirmed and possible azole resistance mechanisms demonstrated in a single series of isogenic isolates is remarkable, indicating the ability of A. fumigatus to adapt in the clinical setting.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>21876055</pmid><doi>10.1128/AAC.00517-11</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antifungal Agents - pharmacology aspergillosis Aspergillus fumigatus Aspergillus fumigatus - drug effects Aspergillus fumigatus - genetics Aspergillus fumigatus - metabolism Azoles Azoles - pharmacology cytochrome P-450 Cytochrome P-450 Enzyme System Cytochrome P-450 Enzyme System - genetics Cytochrome P-450 Enzyme System - metabolism DNA Transposable Elements - genetics Drug Resistance, Fungal - genetics Fungal Proteins Fungal Proteins - genetics Fungal Proteins - metabolism gene duplication gene expression gene expression regulation genes Mechanisms of Resistance messenger RNA microsatellite repeats multiple drug resistance patients Polymorphism, Single Nucleotide Polymorphism, Single Nucleotide - genetics promoter regions Promoter Regions, Genetic - genetics resistance mechanisms Saccharomyces cerevisiae single nucleotide polymorphism start codon stress response transporters transposons |
title | Interrogation of Related Clinical Pan-Azole-Resistant Aspergillus fumigatus Strains: G138C, Y431C, and G434C Single Nucleotide Polymorphisms in cyp51A, Upregulation of cyp51A, and Integration and Activation of Transposon Atf1 in the cyp51A Promoter |
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